| Starts: | Thursday November 12, 2009 at 1:30pm |
|---|---|
| Ends: | Thursday November 12, 2009 at 2:30pm |
| Event Type: | Training/Seminar |
| Location: | This is a virtual event. |
| Price: | |
| Website: | http://www.EduQuest.net |
| Industry: | medical device |
| Keywords: | Pharmaceutical, Biopharmaceutical, 483, Drug Manufacturer, Quality Systems, Fda, Medical Devices, Compliance, Eduquest, Supply Chain, Warning Letter |
| Intended For: | Quality Systems, Quality Assurance, Regulatory Affairs, Regulatory Compliance, Validation, Auditing, R&D, Engineering, Supply Chain Management |
| Organization: | Designed for Pharmaceutical, Biologics, and Medical Device Companies |
One-Hour FDA Management Audio Briefing, including Q&A session. Covers: What you can expect from the new FDA management team - How FDA's increased emphasis on Quality Systems and Risk impacts your operations - The push towards international rules harmonization -- mirage or reality? - How FDA plans to monitor supply chains and outsourced operations - Lessons learned from recent 483s and Warning Letters - Steps you should take today to prepare for the changes ahead. Presented by Gordon B. Richman, Vice President of Strategic Compliance for EduQuest -- a global team of FDA compliance experts.
Contact me through LinkedIn or at MartinHeavner@Eduquest.net if you would like to receive an invitation to this free November 12 FDA Audio Briefing. Time will be 1:30 - 2:30 pm Eastern Time/12:30 - 1:30 pm Central.